Variant report

Variant	rs10821083
Chromosome Location	chr9:95951477-95951478
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:95896311..95898425-chr9:95950555..95953010,2	MCF-7	breast:
2	chr9:95951384..95953897-chr9:95957626..95959182,2	K562	blood:

Variant related genes	Relation type
ENSG00000131669	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10761199	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10821086	0.87[ASW][hapmap];0.82[CHB][hapmap];0.86[LWK][hapmap];0.95[MKK][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes]
rs10992669	0.84[CHB][hapmap];0.94[YRI][hapmap];0.96[AFR][1000 genomes]
rs10992671	0.80[TSI][hapmap]
rs1106024	0.84[AFR][1000 genomes]
rs1109496	0.88[AFR][1000 genomes]
rs1125029	0.85[CHB][hapmap];0.89[JPT][hapmap]
rs12000524	0.80[CEU][hapmap]
rs12349094	0.83[AFR][1000 genomes]
rs1317698	0.82[MEX][hapmap]
rs1962428	0.89[AFR][1000 genomes]
rs2040093	0.95[YRI][hapmap];0.96[AFR][1000 genomes]
rs2040094	0.95[YRI][hapmap];0.96[AFR][1000 genomes]
rs2154079	0.80[CEU][hapmap];0.80[TSI][hapmap]
rs4524855	0.95[AFR][1000 genomes]
rs4744188	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7846729	0.89[CHB][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes]
rs7856802	0.88[AFR][1000 genomes]
rs7857039	0.81[CHB][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes]
rs7857937	0.87[ASW][hapmap];0.82[CHB][hapmap];0.82[LWK][hapmap];0.93[MKK][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv893580	chr9:95855100-96099377	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv824983	chr9:95902154-95978408	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv430082	chr9:95905745-96095045	Genic enhancers Enhancers Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv614880	chr9:95930572-95978265	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:50 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95947800-95951800	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr9:95948200-95958400	Weak transcription	Lung	lung
3	chr9:95948400-95955200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:95948800-95953000	Enhancers	Right Ventricle	heart
5	chr9:95948800-95955000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:95948800-95955800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr9:95949200-95955800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr9:95949600-95951600	Enhancers	Brain Hippocampus Middle	brain
9	chr9:95949600-95955600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr9:95949800-95951600	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr9:95949800-95952000	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr9:95949800-95954600	Weak transcription	Right Atrium	heart
13	chr9:95950000-95951600	Enhancers	Brain Anterior Caudate	brain
14	chr9:95950000-95952000	Enhancers	Rectal Smooth Muscle	rectum
15	chr9:95950000-95953000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr9:95950000-95953800	Enhancers	Left Ventricle	heart
17	chr9:95950000-95954000	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr9:95950000-95960800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:95950200-95951600	Enhancers	Colon Smooth Muscle	Colon
20	chr9:95950200-95951600	Enhancers	Stomach Mucosa	stomach
21	chr9:95950200-95954000	Enhancers	Pancreas	Pancrea
22	chr9:95950400-95951800	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr9:95950400-95953000	Genic enhancers	Brain Germinal Matrix	brain
24	chr9:95950400-95953200	Weak transcription	Spleen	Spleen
25	chr9:95950400-95953200	Weak transcription	HepG2	liver
26	chr9:95950400-95953800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:95950400-95955000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr9:95950400-95955000	Weak transcription	Fetal Intestine Large	intestine
29	chr9:95950400-95955200	Weak transcription	Gastric	stomach
30	chr9:95950600-95951800	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr9:95950600-95955000	Strong transcription	Fetal Intestine Small	intestine
32	chr9:95950800-95951600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr9:95950800-95951800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:95950800-95951800	Enhancers	Brain Cingulate Gyrus	brain
35	chr9:95950800-95967400	Enhancers	Fetal Heart	heart
36	chr9:95951000-95951600	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr9:95951000-95951800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr9:95951000-95951800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr9:95951000-95952000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:95951000-95952000	Enhancers	Brain Angular Gyrus	brain
41	chr9:95951200-95951600	Enhancers	H9 Cell Line	embryonic stem cell
42	chr9:95951200-95951600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr9:95951200-95951600	Weak transcription	Psoas Muscle	Psoas
44	chr9:95951200-95951800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr9:95951200-95952600	Weak transcription	Fetal Brain Male	brain
46	chr9:95951200-95954600	Weak transcription	Fetal Thymus	thymus
47	chr9:95951200-95955000	Weak transcription	Colonic Mucosa	Colon
48	chr9:95951200-95955000	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr9:95951400-95951600	Enhancers	Duodenum Mucosa	Duodenum
50	chr9:95951400-95952200	Enhancers	Fetal Brain Female	brain

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